The Clinovia 4-Step Placement Framework
How we prepare every scholar to clear technical interviews with multinational CROs.
Resume Re-Engineering
Transforming academic CVs into clinical trial dossiers highlighting live hospital rotation hours, EDC tools, and GCP compliance.
Technical Mock Drills
Rigorous mock interviews conducted by active industry practitioners from TCS, IQVIA, and Novartis covering real case scenarios.
Corporate Pool Drives
Direct access to recruitment drives hosted exclusively for Clinovia students and Central India life science graduates.
Offer & Onboarding
Guidance on CTC negotiation, employment documentation, and post-placement continuous professional development support.
Current Openings at Clinovia Research
Grow with Central India's fastest-expanding clinical research and evidence generation organization.
Clinical Research Coordinator (CRC)
Location: Partner Multispecialty Hospitals, Nagpur | Experience: 1–3 Years
Manage day-to-day operations of Phase II–IV trials across hospital wards, subject recruitment, informed consent administration, and Investigator Site File (ISF) maintenance.
- Execute patient screening, ICF documentation, and trial visits
- Maintain Investigator Site Files (ISF) in audit-ready status
- Coordinate with hospital floor nurses and principal investigators
- B.Pharm / M.Pharm / MSC/BSc Life Sciences degree with Clinical trial Diploma/certification
Clinical Data Associate (EDC / CDM)
Location: Clinovia Central Office, Nagpur | Experience: 1–2 Years
Execute electronic data entry, discrepancy review, query resolution, and reconciliation using Oracle InForm and Medidata Rave environments.
- Review eCRFs and perform manual data discrepancy checks
- Assist lead data manager with database lock activities and SAE reconciliation
- Knowledge of CDISC SDTM nomenclature and MedDRA terminology
Medical Writer (Clinical Reports)
Location: Hybrid / Remote | Experience: 2+ Years
Draft ICH-GCP compliant clinical study reports (CSRs), observational study protocols, and peer-reviewed journal manuscripts for PubMed/Scopus indexing.
- Author clinical protocols, investigator brochures, and CSR modules
- Scientific communication for biomedical trials and regulatory dossiers
- Mastery of AMA style manual and ICMJE disclosure standards
Senior Research Fellow (SRF) (AYUSH)
Location: Remote | Experience: 6 Months
Lead clinical study coordination, protocol execution, and ethical review procedures for integrative AYUSH and traditional healthcare trials.
- Knowledge of GCP, Execution of Clinical Trial Protocol, Understanding of IEC procedures
- BAMS/MD (Ayurveda), BDS, MDS, BPTH, MPTH with Clinical trial certification/Diploma
Drug Safety Associate (Pharmacovigilance)
Location: Pune / Hyderabad | Experience: 0–2 Years
Triage adverse events, author safety narratives, process Individual Case Safety Reports (ICSRs), and perform MedDRA coding.
- MBBS/BHMS/BAMS/MD (Ayurveda), BDS, MDS, BPTH, MPTH with Pharmacovigilance certification/Diploma
- Strong medical terminology, adverse event causality assessment, and regulatory submission understanding
Scientific Writers
Location: Online / Hybrid | Experience: 1–3 Years
Author research writing manuscripts, clinical protocols, systematic reviews, and thesis/dissertation documentation for peer-reviewed indexed publications.
- MD (Ayurveda), MDS, MPTH, M.Pharm, MPH, MCom, MSc with excellent publication record and scientific writing skills
- Proven track record in PubMed/Scopus articles, medical literature synthesis, and biostatistical interpretation
Submit Your Application
Apply for upcoming campus recruitment drives, internal Clinovia vacancies, or student placement registry.
Careers Cell
Email: careers@clinovia.in
Phone: +91 712 299 8877
Wardha Road, Medical Corridor, Nagpur, Maharashtra 440015, India
Job / Drive Application Form
Please provide your credentials and role preference.